Photocatalytic degradation of CI Acid Red 27 by immobilized ZnO on glass plates in continuous-mode

被引:96
作者
Behnajady, M. A.
Modirshahla, N.
Daneshvar, N.
Rabbani, M.
机构
[1] Islamic Azad Univ, Dept Appl Chem, Res Lab, Tabriz Branch, Tabriz, Iran
[2] Univ Tabriz, Fac Chem, Dept Appl Chem, Water & Wastewater Treatment Res Lab, Tabriz, Iran
[3] Islamic Azad Univ, Dept Appl Chem, Fac Chem, N Tehran Branch, Tabriz, Iran
关键词
advanced oxidation processes (AOPs); UV/ZnO; heterogenous photocatalysis; immobilized ZnO catalyst; decolorization; continuous-flow photoreactor; CI acid red 27;
D O I
10.1016/j.jhazmat.2006.07.054
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The photocatalytic degradation of C.I. Acid Red 27 (AR27), an anionic monoazo dye of acid class, in aqueous solutions was investigated with immobilized ZnO catalyst on glass plates in a continuous-mode. In the slung ZnO system the separation and recycling of the photocatalyst is practically difficult. Thus, ZnO was immobilized on solid supports to solve this problem. The removal percent increases with increasing the photoreactor volume and light intensity but it decreases when the flow rate is increased. With decreasing flow rate from 43 to 15 ml min(-1), the complete decolorization and degradation was obtained at around 748 and 1080cm(3) from photoreactor volume. The increase in the light intensity from 21.4 to 58.5 W m(-2) increases the decolorization from 23 to 57.6% and degradation from 17.5 to 37.8% for 374 cm 3 of photoreactor volume. NH4+, NO3-, NO2- and SO42- ions were analyzed as mineralization products of nitrogen and sulfur heteroatoms. Results showed that final concentration of SO42- ions and N-containing mineralization products were less than the finally expected stoichiometric values. The positive slope of production of NH4+, NO3- and NO2- shows that these compounds are initial products resulting directly from the initial attack on the nitrogen-to-nitrogen double bond (-N=N-) of the azo dye. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:257 / 263
页数:7
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